Clinical features and underlying genetic causes in neonatal encephalopathy: A large cohort study-Reference-Cited by-同舟云学术

Clinical features and underlying genetic causes in neonatal encephalopathy: A large cohort study

Published:2020-09-04 Issue:4 Volume:98 Page:365-373
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Yang Lin¹^ORCID,Chen Xiang²,Liu Xu²,Dong Xinran³,Ye Chang²,Deng Dongli²,Lu Yulan³,Lin Yifeng³,Zhou Wenhao¹²³⁴⁵^ORCID

Affiliation:

1. Clinical Genetic Center Children's Hospital of Fudan University Shanghai China

2. Department of Neonatology Children's Hospital of Fudan University Shanghai China

3. Key Laboratory of Birth Defects Children's Hospital of Fudan University Shanghai China

4. CAS Center for Excellence in Brain Science and Intelligence Technology (CEBSIT), Shanghai Institute of Biological Sciences, Chinese Academy of Sciences Shanghai China

5. MOE Frontiers Center for Brain Science Fudan University Shanghai China

Funder

National Natural Science Foundation of China

Health and Family Planning Commission of Sichuan Province

Shanghai Shen Kang Hospital Development Center

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13818

Reference40 articles.

1. Executive Summary

2. Intrapartum-related neonatal encephalopathy incidence and impairment at regional and global levels for 2010 with trends from 1990

3. Cognitive Outcomes After Neonatal Encephalopathy

4. Management and investigation of neonatal encephalopathy: 2017 update

5. Prospective cohort study for identification of underlying genetic causes in neonatal encephalopathy using whole-exome sequencing

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